Sulfanilamide → 4-(4-(4-(Aminomethyl)piperidin-1-yl)furo[3,2-d]pyrimidin-2-ylamino)benzenesulfonamide
Reaction equation
[C:1]([N:5]([C:2](=[O:3])[O-:4])[CH2:9][CH:10]1[CH2:11][CH2:12][N:13]([c:16]2[c:17]3[c:18]([n:19][c:20]([NH:22][c:23]4[cH:24][cH:25][c:26]([S:29]([NH2:30])(=[O:31])=[O:32])[cH:27][cH:28]4)[n:21]2)[cH:33][cH:34][o:35]3)[CH2:14][CH2:15]1)([CH3:6])([CH3:7])[CH3:8].[C:47]([O:48][C:49]([NH:50][CH2:51][CH:52]1[CH2:53][CH2:54][NH:55][CH2:56][CH2:57]1)=[O:58])([CH3:59])([CH3:60])[CH3:61].[Cl:36][c:37]1[n:38][c:39]([Cl:40])[c:41]2[o:42][cH:43][cH:44][c:45]2[n:46]1.[Cl:80][CH2:81][Cl:82].[F:73][C:74]([F:75])([F:76])[C:77]([OH:78])=[O:79].[NH2:62][c:63]1[cH:64][cH:65][c:66]([S:67](=[O:68])(=[O:69])[NH2:70])[cH:71][cH:72]1>>[NH2:5][CH2:9][CH:10]1[CH2:11][CH2:12][N:13]([c:16]2[c:17]3[c:18]([n:19][c:20]([NH:22][c:23]4[cH:24][cH:25][c:26]([S:29]([NH2:30])(=[O:31])=[O:32])[cH:27][cH:28]4)[n:21]2)[cH:33][cH:34][o:35]3)[CH2:14][CH2:15]1Participants
7
Reactant 6
Product 1
Sources & evidence
- ORD record
- ord-5ff71911191b4aa3b84a8a5e6dfb9568
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (3/10)
Reaction notes
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